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Lsss

FDA UDI

Class I (US FDA UDI)

by Lockdown Medical Ltd

Identity

Trade Name
LSSS FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
AO SCREWDRIVER SHAFT Ø2.5MM (HEX). THE FINISHED PART NUMBER IS IN629/1 - "AO SCREWDRIVER SHAFT Ø2.5MM (HEX) - RM04051" FDA UDI
Model / Reference
RM04051 FDA UDI
Description
AO SCREWDRIVER SHAFT Ø2.5MM (HEX). THE FINISHED PART NUMBER IS IN629/1 - "AO SCREWDRIVER SHAFT Ø2.5MM (HEX) - RM04051" FDA UDI

Identifiers

Catalog Number
RM04051 FDA UDI
Primary DI / UDI-DI
05060433600777 FDA UDI
FDA Product Code
MDM FDA UDI
LRZ FDA UDI
HXX FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical screwdriver, reusable

Lsss by Lockdown Medical Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2cec63f0-67c5-4a8e-a1c8-3e07406ff152 34 fields · synced Jun 6, 2026